GSK
Patricia Tuyaret is an experienced professional in clinical quality assurance and regulatory compliance, currently serving as Associate Director of Clinical Quality Assurance for Third Party Program Management at GSK since June 2023. Previously, Patricia held various positions at Bristol Myers Squibb from 1997 to October 2022, including Director of Data and Vendor Quality and Associate Director of Vendor Audit Strategy, where initiatives led to improved clinical vendor oversight and quality processes. Early career roles included regulatory compliance manager and auditor, contributing to successful audits and inspections worldwide. Patricia commenced her career as a Clinical Research Associate at Novo Nordisk and previously worked in scientific media as a journalist. Educational qualifications include a Master's degree in Business Administration from IAE France and a degree from Université Paul Sabatier Toulouse III.
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